FDA Label Search
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NDC Search Results on Proprietary Name: tramadol
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Proprietary Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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Tramadol Hydrochloride | 43353-072-72 | Aphena Pharma Solutions - Tennessee, LLC | ANDA076003 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE | 61919-073-90 | DIRECT RX | ANDA076003 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 68387-497-12 | Keltman Pharmaceuticals, Inc. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 21695-236-50 | Rebel Distributors Corp. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 21695-236-30 | Rebel Distributors Corp. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 68387-497-20 | Keltman Pharmaceuticals, Inc. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 21695-236-60 | Rebel Distributors Corp. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 68387-497-90 | Keltman Pharmaceuticals, Inc. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 21695-236-72 | Rebel Distributors Corp. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 21695-236-20 | Rebel Distributors Corp. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 68387-497-30 | Keltman Pharmaceuticals, Inc. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
Tramadol Hydrochloride and Acetaminophen | 68387-497-60 | Keltman Pharmaceuticals, Inc. | ANDA076475 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HCL AND ACETAMINOPHEN | 69844-049-01 | Graviti Pharmaceuticals Private Limited | ANDA076914 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HCL AND ACETAMINOPHEN | 69844-049-02 | Graviti Pharmaceuticals Private Limited | ANDA076914 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 50090-3705-2 | A-S Medication Solutions | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-3 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-2 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 57664-537-88 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 52959-814-30 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-7 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-6 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 52959-814-12 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 57664-537-13 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 52959-814-20 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 52959-814-40 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-8 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 71335-0151-1 | Bryant Ranch Prepack | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 68071-2831-2 | NuCare Pharmaceuticals,Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 52959-814-60 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | 57664-537-18 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
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